Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11066194
rs11066194
1 1.000 0.040 12 112212323 intron variant A/G snv 4.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs11066280
rs11066280
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2014 2014
dbSNP: rs2074356
rs2074356
18 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 0.700 1.000 1 2018 2018